Clinical Trial Support
BioRep and Advice Pharma operate synergistically to provide a comprehensive range of Contract Research Organization (CRO) services, supporting clinical trial management, clinical data handling, and biological sample management through a fully integrated model.
With more than 20 years of experience in global biological material logistics, storage, and management, BioRep provides extensive support in the planning, implementation, and execution of sponsor-driven clinical studies.
Its primary clients include:
- Pharmaceutical companies
- Biotechnology companies
- Government institutions
- Foundations
- Universities
Expertise, efficiency, and rapid execution make BioRep a trusted partner for accelerating study start-up timelines and reducing overall project costs.
About Advice Pharma
Advice Pharma is a Contract Research Organization (CRO) that develops innovative solutions leveraging advanced digital technologies. The company specializes in three key areas:
- Clinical Trial Management: Management of clinical studies across multiple therapeutic areas by experienced teams working closely with sponsors throughout the project lifecycle.
- Clinical Research Software: Development of proprietary Electronic Data Capture (EDC) platforms and Clinical Trial Management Systems (CTMS) designed to improve clinical data management while ensuring compliance with Good Clinical Practice (GCP) guidelines.
- Digital Therapeutics:Development and implementation of innovative digital therapeutic solutions.
Integrated CRO Services: A Single Strategic Partner
By combining BioRep’s biobank and laboratory capabilities with Advice Pharma’s proprietary software platforms, sponsors benefit from a fully integrated clinical research ecosystem capable of managing the entire sample lifecycle.
Clinical Research Services
- Study design
- Clinical protocol development
- Clinical project management
- Study start-up activities
- Clinical monitoring
- Medical monitoring
- Regulatory affairs
- Biostatistics
- Clinical study report preparation
Clinical Data Management
- Paper CRF design
- eCRF development
- Clinical database design and management
- Data Validation Plan development
- Data management activities
- Data cleaning
- DCF and query management
Real-World Evidence (RWE)
- Management of clinical data from external sources, including laboratories, health records, and imaging systems
Decentralized Clinical Trials (DCT)
- eConsent solutions
- ePRO platforms
- Connected medical devices
- Remote visits
- Telemedicine services
Full Logistics Services
- End-to-end logistics management of study biological materials
- Distribution of collection kits to national and international study sites
- Collection of biological samples from clinical trial participants
- Full traceability of collection kits and samples through anonymized barcodes integrated with the LIMS platform
- Temperature-controlled storage of post-analysis clinical trial samples within BioRep’s biobank (from +4°C to -196°C)
Customized Collection Kits
- Tailor-made collection kits designed for each clinical trial
- Customized identification labels and unique tracking systems
- Distribution or destruction of biological samples at study completion according to sponsor requirements
Laboratory Services
Integrated laboratory services including:
- Cellular biology
- Molecular biology
- Microbiology
- Genetics
Additional services include:
- Shipment of clinical trial samples to external laboratories worldwide
- Support in preparing Training Manuals for participating clinical study sites